Basic Information

Reference Number

WS4617512505-Doc4941941764

Issuing Organization

Department of Public Works and Government Services (PSPC)

Owner Organization

Department of Public Works and Government Services (PSPC) / Public Health Agency of Canada (PHAC)

Solicitation Type

RFP - Request for Proposal (Formal)

Solicitation Number

WS4617512505

Title

RFP - Manufacture and Supply of Buffered Diluent containing Glycerol and Sterile Empty Vials with Cap Enclosure

Source ID

PWGSC

Agreement Types

Canada-Chile Free Trade Agreement (CCFTA)

Canada-Colombia Free Trade Agreement

Canada-European Union Comprehensive Economic and Trade Agreement(CETA)

Canada-Honduras Free Trade Agreement

Canada-Korea Free Trade Agreement

Canada-Panama Free Trade Agreement

Canada-Peru Free Trade Agreement (CPFTA)

Canadian Free Trade Agreement (CFTA)

Comprehensive and Progressive Agreement for Trans-Pacific Partnership (CPTPP)

North American Free Trade Agreement (NAFTA)

World Trade Organization Agreement on Government Procurement (WTO-AGP)

Canada-UK Trade Continuity Agreement (Canada-UK TCA)

Canada-Ukraine Free Trade Agreement (CUFTA)

Details

Location

National Capital Region

Dates

Publication

2025/01/06 12:00:00 AM EST

Closing Date

2025/02/20 02:00:00 PM EST

Contact Information

Vettoretti, Eric (SPAC/PSPC)

eric.vettoretti@tpsgc-pwgsc.gc.ca

Description

Canada must procure and maintain a stockpile of medical countermeasures (MCM), including diluent and sterile empty glass vials required for vaccination, to support response to Canadian public health emergencies and events.
The Government of Canada has a requirement for the services of a Contractor to manufacture and supply 73,500 vials of a sterile 0.2% phenol, phosphate-citrate based buffered diluent containing 45% glycerol (pH 7.4) in 2 mL labelled vials, accompanied by 11,000 empty 2mL labelled sterile glass vials with a removable cap enclosure system capable of being re-stoppered, in accordance with the technical specifications set out in Appendix A of this solicitation. The diluent and empty vials must be manufactured in accordance with Canada’s Food and Drug Regulations, Part C, Division 2 - current Good Manufacturing Practices (GMP), and be of sufficient quality for use in humans.

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